Issue 11, 2019

A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides

Abstract

A quinine-derived aminophosphine/Ag(I) complex was firstly demonstrated to be an efficient catalyst for the highly stereoselective 1,3-dipolar cycloaddition of azomethine ylides with challenging α,β-unsaturated amide substrates. A wide range of densely functionalized pyrrolidine derivatives containing four contiguous stereogenic centers could be smoothly obtained with excellent diastereo- and enantioselectivities.

Graphical abstract: A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides

Supplementary files

Article information

Article type
Research Article
Submitted
08 Mar 2019
Accepted
12 Apr 2019
First published
15 Apr 2019

Org. Chem. Front., 2019,6, 1879-1884

A AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides

Y. Zhang, Y. You, J. Zhao, X. Zhou, X. Zhang, X. Xu and W. Yuan, Org. Chem. Front., 2019, 6, 1879 DOI: 10.1039/C9QO00347A

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